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24
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0345560177
-
-
note
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[13]
-
-
-
-
25
-
-
0345560179
-
-
note
-
-1]/RT).
-
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28
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0003974162
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National Institute of Standards and Technology, Gaithersburg, MD
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Stein, S.E.1
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0344697944
-
-
2].
-
2].
-
-
-
-
30
-
-
0345128662
-
-
RRD,AnH2.
-
RRD,AnH2.
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-
-
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31
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0001246203
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2307-2312
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L. J. J. Laarhoven, J. G. P. Born, I. W. C. E. Arends, P. Mulder, J. Chem. Soc., Perkin Trans. 2 1997, 2307-2312.
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0345128660
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-
note
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[20]
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36
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0005675110
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-
Halogen exchange is treated in more detail in e.g.: T. Thorstenson, J. Songstad, Acta Chem. Scand. A 1978, 32, 133-139. U. T. Bhalerao, B.C. Raju, P. Neelakantan, Indian J. Chem. 1994, 33B, 1197-1199. A. L. Gemal, J. L. Luche, Tetrahedron Lett. 1980, 21, 3195-3198. A. Clerici, O. Porta, Tetrahedron Lett. 1987, 28, 1541-1544.
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37
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4444315053
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Halogen exchange is treated in more detail in e.g.: T. Thorstenson, J. Songstad, Acta Chem. Scand. A 1978, 32, 133-139. U. T. Bhalerao, B.C. Raju, P. Neelakantan, Indian J. Chem. 1994, 33B, 1197-1199. A. L. Gemal, J. L. Luche, Tetrahedron Lett. 1980, 21, 3195-3198. A. Clerici, O. Porta, Tetrahedron Lett. 1987, 28, 1541-1544.
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Bhalerao, U.T.1
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38
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0001513386
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Halogen exchange is treated in more detail in e.g.: T. Thorstenson, J. Songstad, Acta Chem. Scand. A 1978, 32, 133-139. U. T. Bhalerao, B.C. Raju, P. Neelakantan, Indian J. Chem. 1994, 33B, 1197-1199. A. L. Gemal, J. L. Luche, Tetrahedron Lett. 1980, 21, 3195-3198. A. Clerici, O. Porta, Tetrahedron Lett. 1987, 28, 1541-1544.
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Gemal, A.L.1
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39
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0141551113
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Halogen exchange is treated in more detail in e.g.: T. Thorstenson, J. Songstad, Acta Chem. Scand. A 1978, 32, 133-139. U. T. Bhalerao, B.C. Raju, P. Neelakantan, Indian J. Chem. 1994, 33B, 1197-1199. A. L. Gemal, J. L. Luche, Tetrahedron Lett. 1980, 21, 3195-3198. A. Clerici, O. Porta, Tetrahedron Lett. 1987, 28, 1541-1544.
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Clerici, A.1
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0345128659
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[25]
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[25]
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43
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National Institute of Standards and Technology, Gaithersburg, MD
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44
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0344697941
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[27]
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[27]
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45
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0345128658
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[13]
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[13]
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46
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0041689437
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0344697938
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0344266258
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[25]
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[25]
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50
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0344266257
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[31]
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[31]
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51
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0344697939
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Ed.: Z. Rappoport, Wiley, New York
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52
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0345560167
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[33], p. 427
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[33], p. 427.
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53
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55
-
-
0344697935
-
-
p value (by calculating the frequencies also at 1100 K) because the calculation time was much shorter than that for BrAP.
-
p value (by calculating the frequencies also at 1100 K) because the calculation time was much shorter than that for BrAP.
-
-
-
-
56
-
-
0344697934
-
-
[13]
-
[13]
-
-
-
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57
-
-
0345560174
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[36]
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[36]
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59
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-
0344697932
-
-
Addition of ketyl radicals in 2-propanol to the olefinic moiety in the enol may explain the formation of the side products and is in accordance with the structural elements as detected by GCMS analysis.
-
Addition of ketyl radicals in 2-propanol to the olefinic moiety in the enol may explain the formation of the side products and is in accordance with the structural elements as detected by GCMS analysis.
-
-
-
-
63
-
-
0345128655
-
-
[46] or eliminate a proton yielding styrene. Polymerization of styrene is very fast at the applied temperatures and may render a low mass balance.
-
[46] or eliminate a proton yielding styrene. Polymerization of styrene is very fast at the applied temperatures and may render a low mass balance.
-
-
-
-
65
-
-
0344697931
-
-
note
-
-1, which has been derived from the addition of phenoxyl to styrene, may well be higher for aliphatic systems.
-
-
-
-
66
-
-
0344697930
-
-
unpublished results
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P. Mulder, unpublished results.
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Mulder, P.1
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67
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0000801869
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J. T. Autrey, M. S. Alnajjar, D. A. Nelson, J. A Franz, J. Org. Chem. 1991, 56, 2197.
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68
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0345560172
-
-
[36]
-
[36]
-
-
-
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69
-
-
0344266244
-
-
[1a]
-
[1a]
-
-
-
-
70
-
-
0344266250
-
-
-1.
-
-1.
-
-
-
-
71
-
-
0344697929
-
-
[33], p. 90.
-
[33], p. 90.
-
-
-
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72
-
-
0345560171
-
-
-1.
-
-1.
-
-
-
-
73
-
-
0344266245
-
-
-8 M (see text).
-
-8 M (see text).
-
-
-
-
74
-
-
0344697927
-
-
-1.
-
-1.
-
-
-
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75
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0001557504
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[36]
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79
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0004133516
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